Methods: ProRoot MTA (Dentsply Tulsa, Tulsa, OK, USA) and a white Portland cement (Mapei, Italy) were mixed and left to set 24h. MSCs were cultured on the samples in the presence and absence of osteogenic medium and observed after 5 days by confocal scanning laser microscopy (CSLM) using the cytoskeleton marker phalloidin. Cell proliferation was evaluated by means of alamar blue assay after 1, 3, 5 and 7 days, using cells seeded on polystyrene culture wells as controls. In order to assess the effect on migratory ability of MSCs a transwell migration assay was performed for 18 h positioning MTA and Portland cements in 6-well plates and the cells in 8 μm pore inserts. The surface topography of cements was evaluated by atomic force microscopy.
Results: MSCs observed under CLSM showed proliferation and spread, forming a continuous layer on the upper surface of the MTA. Cells grown in osteogenic medium were bigger with a flat and polygonal shape. Cell proliferation was significantly higher on MTA than on Portland cement with an increase of 60% of the control after 1 and 3 days, while the peak of proliferation was reached after 5 days. Moreover, MTA was able to enhance cell migration significantly more than Portland cement. Finally, AFM images of MTA surface showed nanostructured features.
Conclusions: MTA was able to promote MSCs adhesion, proliferation and differentiation.
Acknowledgements: This study was supported by PRIN 2007M9YTFJ_003 and Rete Nazionale di Ricerca TissueNet RBPR05RSM2 from MIUR.